Canonical Allele Identifier: CA406381018
Community Standard Title: NC_000019.10:g.45529088C>A
Gene: OPA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45529088C>A , CM000681.2:g.45529088C>A GRCh38
NC_000019.9:g.46032346C>A , CM000681.1:g.46032346C>A GRCh37
NC_000019.8:g.50724186C>A NCBI36
NG_013332.1:g.60777G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001017989.2:c.511G>T NP_001017989.2:p.Ala171Ser
NM_001017989.3:c.511G>T NP_001017989.2:p.Ala171Ser
ENST00000323060.3:c.511G>T ENSP00000319817.3:p.Ala171Ser
ENST00000323060.4:c.511G>T ENSP00000319817.3:p.Ala171Ser
XM_011527348.1:c.352G>T XP_011525650.1:p.Ala118Ser